HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838523Generated: October 31, 2026
Potassium Carbonate → 4-(3-Acetoxy-4-methylanilino)-6-methoxy-7-(2-methoxyethoxy)quinazoline
https://huagongshe.com/reaction/1838523
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | 4-(3-Acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline | HCID 135450804 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Acetoxy-4-methylanilino)-6-methoxy-7-(2-methoxyethoxy)quinazoline | HCID 22478233 | 84.3% |
Reaction Steps
Potassium carbonate (2.2 g, 16 mmol) was added to a solution of 4-(3-acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline (1.51 g, 4 mmol) in DMF (30 ml) and the mixture stirred for 15 minutes. 2-Bromoethyl methyl ether (667 mg, 4.8 mmol) was then added dropwise. The mixture was stirred for 1 hour at ambient temperature, then heated at 60° C. for 17 hours and finally allowed to cool. The insoluble material was removed by filtration and the filter pad washed with DMF. The filtrate was partitioned between ethyl acetate and water, the organic layer was separated, washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5 followed by 93/7). The purified product was triturated with ether to give 4-(3-acetoxy-4-methylanilino)-6-methoxy-7-(2-methoxyethoxy)quinazoline (1.34 g, 84%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06673803B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-8f9d1fdf2f8d41bb8aad3698f5ce8ca4 |
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| Source note | uspto-grants-2004_01 |
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